Method for estimating blood component quantities in surgical textiles

ABSTRACT

Systems and methods for detecting, counting and analyzing the blood content of a surgical textile are provided, utilizing an infrared or depth camera in conjunction with a color image.

CROSS-REFERENCE TO RELATED APPLICATIONS

This Application is a continuation of U.S. patent application Ser. No.15/390,017, filed on Dec. 23, 2016, which claims priority to U.S.Provisional Patent Application No. 62/387,222, filed on Dec. 23, 2015.This Application is also related to U.S. patent application Ser. No.13/544,664, filed on Jul. 9, 2012, which is incorporated in its entiretyby this reference in its entirety.

TECHNICAL FIELD

This invention relates generally to the field of blood loss managementand more specifically to a new and useful method for estimating bloodcomponent quantities in surgical textiles in the field of blood lossmanagement.

SUMMARY

This invention relates generally to the field of blood loss managementand more specifically to a new and useful method for estimating bloodcomponent quantities in surgical textiles in the field of blood lossmanagement. Systems and methods for detecting, counting and analyzingthe blood content of a surgical textile are provided, utilizing aninfrared or depth camera in conjunction with a color image.

In one example, a system for measuring blood content is provided,comprising a color imaging system configured to acquire color images, aninfrared imaging system, to acquire infrared images, a processorconfigured to identify a surgical textile shape using the infraredimages, generate shape information from the infrared images, use theshape information to identify surgical textile pixels in the colorimages, and extract blood information from the surgical textile pixels.The processor may be further configured to transform the infrared imagesto a coordinate system corresponding to the color images, to generate ata depth image from one of the infrared images, to identify a planar setof pixels in the depth image, and/or to detect a surgical textile imageperimeter in the depth image. The detection of the surgical textileimage perimeter may be performed by looking for a sharp vertical depthdrop-off in the depth image. The processor may be further configured todownsample the depth image or the infrared image, to generate a maskimage from the downsampled depth image, to upsample the mask image, toperform fill-in of missing infrared pixel region in the infrared images,to generate a mask image using the detected perimeter, and/or totransform the mask image to a coordinate system of the color images. Thedetected perimeter may be a top edge and a bottom edge of a surgicaltextile image, or may be opposing edges of a surgical textile image,and/or corners of a surgical textile image.

In another example, a method of analyzing an object containing a bloodcomponent is provided, comprising acquiring a depth image and a colorimage of an object containing a blood component, using the depth imageto determine the presence of the object in a field of view, using thecolor image to estimate the a blood component characteristic. The methodmay further comprise generating an image mask using the depth image, andapplying the image mask to the color image to eliminate backgroundpixels. The method may further comprise applying at least one of erosionand dilation image processing to the depth image.

In still another example, a method for estimating a fluid componentquantity in surgical textiles is provided, comprising capturing a firstinfrared image of a field of view at a first time, detecting a shape orsurface characteristic of a surgical textile in the first infraredimage, indexing a frame counter upon detecting the shape or surfacecharacteristic in the first infrared image, capturing a second infraredimage of the field of view at a second time succeeding the first time,detecting a surface characteristic of a surgical textile in the secondinfrared image, indexing the frame counter upon detecting the shape orsurface characteristic in the second infrared image, and indexing anon-detection counter upon a failure to detect a shape or surfacecharacteristic of a surgical textile in the second infrared image. Themethod may further comprise clearing the frame counter and thenon-detection counter upon reaching a pre-specified value. The methodmay further comprise comparing the frame counter to a threshold value,capturing a color image of the field of view if the frame counter may beequal to or exceeds the threshold value, transforming a region of thecolor image corresponding to a surgical textile into an estimation of ablood component quantity, and clearing the frame counter. The method mayfurther comprise generating an image mask using the second infraredimage, and using the image mask with the color image to identify theregion of the color image corresponding to the surgical textile.

In another example, a method of performing fluid monitoring is provided,comprising capturing an infrared image of a field of view, capturing acolor image of the field of view, generating an image mask using theinfrared image, and using the image mask with the color image toidentify a region of the color image corresponding to a surgicaltextile. The method may further comprise transforming the infrared imageto the geometry perspective of the color image. The method may furthercomprise downsampling the infrared image prior to generating the imagemask. The method also may further comprise upsampling the image maskbefore using the image mask to identify the region of the color image.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 is a flowchart representation of a method for analyzing asurgical textile; and

FIG. 2 is a flowchart representation of one variation of the method forclassifying and counting a surgical textile for certain characteristics;

FIG. 3 is a schematic representation of an exemplary depth imagingsystem;

FIG. 4 depicts an exemplary computing device and user display,highlighting the surgical textile;

FIG. 5 is a flowchart representation of a method of detecting removal ofa surgical textile from the field of view;

FIG. 6 is a flowchart representation of a method of de-skewing andreassessing an image;

FIG. 7 is a flowchart representation of a method for generating an imagemask; and

FIG. 8 is another flowchart representation of a method for generating animage mask using erosion and dilation processing.

DESCRIPTION OF THE EMBODIMENTS

Overestimation and underestimation of patient blood loss is asignificant contributor to high operating and surgical costs forhospitals, clinics and other medical facilities. Specifically,overestimation of patient blood loss results in wasted transfusion-gradeblood and higher operating costs for medical institutions and can leadto blood shortages. Underestimation of patient blood loss is a keycontributor of delayed resuscitation and transfusion in the event ofhemorrhage and has been associated with billions of dollars in avoidablepatient infections, re-hospitalizations, and lawsuits annually. Thus,there is a need in the surgical field for a new and useful system andmethod for estimating extracorporeal blood volume in a physical sample.

The systems and methods described herein utilize a color camera systemto acquire images of surgical textiles or other operating room surfacesand to estimate the blood content in each image. In addition, the systemcan also track the number of surgical textiles used during a procedure,to assist the surgical or procedure staff with confirming that allsurgical textiles were accounted for, and not left in the patient, priorto surgical closure. The surgical textiles may include items such as anabsorbent surgical gauze sponge, a surgical dressing, a surgical towel,surgical gown, scrubs or other clothing, a table, bed or bed sheet,wall, floor surface, an external skin surface, a surgical glove, asurgical implement, or any other surface, material, substrate, orobject.

To facilitate the presentation of objects to the color camera system forassessment and/or counting, an infrared or other type of cameraconfigured to provide depth information may be used to detect thepresentation of the object for analysis. Depth information from such asystem may more easily distinguish the object, which is located in theforeground, from other objects not intended to be analyzed, and will belocated in the background. Examples of optical systems that can providedepth information include range-gated time-of-flight (ToF) cameras,RF-modulated ToF cameras, pulsed light ToF, and projected light stereocameras, etc.

To improve the accuracy of the detection process, other features of theobject may also be detected to reduce the risk of false positiveresults. The reliability of the detection process may also be improvedby identifying the presence of the object in multiple consecutive framesbefore analyzing the object and presenting the results.

1. Applications

Generally, as depicted in FIG. 1, the various methods described hereinmay be executed by a computing device 100 to acquire one or more images102 using an optical sensor system 104 to detect a surgical textile 106a, such as a surgical gauze, a surgical sponge, or a surgical towel, inthe field of view 108, as depicted in S110. In S111, the image 102 isanalyzed to confirm the presence of the surgical textile (image) 106 bover a sequence of frames output by the optical sensor system in S111,and to automatically capture a color image 110 of the surgical textile106 b in S125 once its presence is confirmed, or utilize the last colorimage concurrently captured with images 102. The computing device 100can then index a local surgical textile counter 112 in S150, and in S140locally transform color values of pixels in the color image 110 into anestimation of an amount of a blood component (e.g., a mass ofhemoglobin, a volume of whole blood) in the surgical textile 106 b, orpass the color image 110 to a remote computer system for suchprocessing.

In particular, the computing device 100 may be configured to detect apossible surgical textile image 106 in a first frame (e.g., an infraredimage) and to index a frame counter 114 according in Block S112, and toindex the frame counter 114 again if a possible surgical textile 106 isagain detected in the subsequent frame, or to clear the frame counter114 in Block S130 if a surgical textile image 106 b is not detected inthe next frame. This process is repeated and the frame counter 114 isindexed for as a long as a possible surgical textile 106 b is detectedin subsequent frames and until the frame counter 114 contains a valueequivalent to a threshold value 116. Once the frame counter contains avalue equivalent to a threshold value 116, the computing device canrecord a color image 110 of the surgical textile 106 and process thecolor image 110 to determine its content of a blood component (e.g.,hemoglobin) in Block S140 and/or to update a textile counter 112 for thedetected surgical textile 106 in Block S150. For example, the computingdevice 100 can implement a threshold value 116 of “7,” which correlatesto seven consecutive frames containing a region determined to likelycorrespond to a surgical textile 106, and the computing device 100 cancapture a digital color photographic image 110 of a surgical textile 106b once the frame counter 114 contains a value of “7” and process thisimage 110 to determine the mass or volume of hemoglobin or whole bloodcomponent in the surgical textile 106. In other examples, the thresholdvalue may be set in the range of about 3 to about 100, or about 5 toabout 70, or about 30 to about 50, or about 8 to about 20. By tracking asurgical textile 106 through a sequence of frames and only confirmingthe presence of the surgical textile 106 b if the surgical textile 106 bis detected in a minimum number of consecutive frames, the computingdevice 100 may minimize or eliminate false positive confirmations ofsurgical textiles 106 b, thereby minimizing or eliminating erroneoustextile counter events and automated collection and processing of imagesthat do not contain surgical textiles. This tracking process may alsoimprove computational efficiency, by reducing the need to perform bloodcontent determination of every color image.

In further embodiments, the computing device 100 may also be configuredto automatically detect a surgical textile 106 a within its field ofview 108 (i.e., within the field of view of one or more optical sensorsof the optical sensor system 104 integrated into and/or connected to thecomputing device 100), thereby reducing or eliminating need for the userto manually trigger capture of a bloodied surgical textile, such asdepression of a foot pedal, touch control, gesture control or voicecontrol. Furthermore, the computer system 100 may be configured toprovide real-time visual feedback though an integrated or connecteddisplay 118, such as a visual indicator that a surgical textile 106 a isdetected within the field of view 108 of the computing device 100, thatan image of the surgical textile was captured, and/or a prompt tomanipulate the surgical textile 106 a to yield a sufficient orhigher-quality image.

The methods described herein may be executed locally by the computingdevice 100 installed or arranged within an operating room, a deliveryroom, an ambulance, or in any other medical or emergency response spaceor unit. However, the method may also be executed locally and/orremotely, such as by a remote server. Blocks of the method are describedherein as detecting surgical sponges and capturing and processing imagesof surgical sponges. However, Blocks of the method can additionally oralternatively be implemented to detect surgical gauzes, surgical towels,or any other textile and to capturing and processing images of suchtextiles.

2. Exemplary Methods

As shown in FIG. 1, a general method S100 for estimating blood componentquantities in surgical textiles comprises, at a first time point, usingthe optical system 104 to capture a first infrared or depth image 102 ofa field of view 108 in Block S110. In this particular example, theoptical system 104 comprises a computing device 100 with a built-indisplay 118 and a color camera or color imaging system 120 on the sameside of the computing device display 118, but in other examples thecomputing device 100 may be configured to use a camera on the oppositeside of the display 118. To capture the depth image 102, an infraredcamera or depth imaging system 122 is directly mounted on the computingdevice 100, but in other examples the depth imaging system 122 may bemounted at a location spaced apart from the computing device 100. Insome variations, the infrared or depth camera 120 is configured to bemounted to a specific computing device 100 such that the optical axis ofthis second camera 121 is aligned vertically and parallel to the opticalaxis of the color camera 120. In other examples, however, the opticalaxis of the second camera 121 may be aligned with the horizontal axis ofthe color camera 120, or may not be aligned with either axis of thecolor camera. The second camera 122 may alternatively be configured tointersect the optical axis of the color camera 120 at a location that isat a distance in the range of about 15 cm to 200 cm, or about 30 cm toabout 100 cm, from the color camera 120.

The image 102 is then analyzed at S111 to detect a surface or shapecharacteristic corresponding to a surgical textile 106 b in the firstinfrared image 102. If the presence of a surgical textile 106 b isconfirmed, a frame counter 114 is indexed in S112. At a second orsubsequent time point succeeding the first time point, a second orsubsequent infrared image 102 of the field of view 108 is captured, andin response to detecting a surface or shape characteristic of a surgicaltextile 106 b in the second or subsequent infrared image 102, indexingthe frame counter 114 again. This detection is performed repeatedlyuntil either a threshold value 116 is reached, or in response to failureto detect a surface or shape characteristic of a surgical textile in thesecond or a subsequent infrared image, clearing the frame counter inS130. Upon the frame counter containing a value equivalent to athreshold value at S113, a color image 110 of the field of view 108 maybe captured by the color camera 120. In variations wherein color imagesare taken with the infrared or depth images 102, the last color image110 from those taken during Block S110 or S111 may be used. The regionsof the color image 110 corresponding to the surgical textile 106 b areidentified, and then those regions are further analyzed to identify theportions containing blood. Those portions are then transformed into anestimation of a blood component quantity in Block S140. The system thenclears the frame counter in S130.

Further variations of the method are also depicted in FIG. 1. Forexample, at a first time point, when a first image 102 of a field ofview 100 is captured by the optical system 104 in S110, and a renderedform of the first image 102 may be provided on a display 118 in S120.This displayed image 102 may correspond to a depth image or a colorimage. In response to detecting a first surface or shape characteristicof a surgical textile 106 b in the first image 102, a frame counter 114is indexed in in S112 and, on the display 118, highlighting a region ofthe first image 102 corresponding to the first surface or shape of thesurgical textile 106 b in Block S122. This variation of the method mayalso include, at a second or subsequent time point succeeding the firsttime point, capturing a second or subsequent image 102 of the field ofview 108, rendering a form of the second or subsequent image 102 on thedisplay 118; and, in response to detecting a second surface or shapecharacteristic of a surgical textile 106 b in the second image 102,indexing the frame counter 114 at S112 and, on the display 118,highlighting a region of the second image 102 corresponding to thesecond surface or shape based on a value of the frame counter 114 atS122. Upon a failure to detect a second surface or shape characteristicof a surgical textile 106 b in the second or subsequent image 102, theframe counter 114 is cleared in S130, or in response to the framecounter 114 containing a value equivalent to a threshold value 116,indexing a textile counter 112 in Block S150 and clearing the framecounter 114. In procedures or surgeries utilizing different surgicaltextiles, multiple surgical textile counters may be provided, and thecounter for the corresponding surgical textile 106 may be indexed inS150.

3. System

As shown in FIG. 1, the computing device 100 includes an imaging system104 defining a field of view 108 and configured to capture depth andcolor data from its field of view 108. In particular, the computingdevice 100 can include a depth imaging camera or system 122 that outputsdepth information or maps 102 of the field of view 108 and a colorimaging camera or system 120 that outputs color images 110 of the fieldof view 108.

As show in FIG. 3, in one implementation, the depth imaging system 122includes a housing 300 with a structured light infrared (“IR”) projector302 that defines a projection field of view and projects infrared lightin a pattern of dots into projection field of view, an IR camera 304that defines an infrared field of view substantially similar to theprojection field of view and configured to capture a sequence ofinfrared images (or “infrared frames”) of the infrared field of view;and an internal processor 306 configured to transform a distorted dotpattern detected by the IR camera 304 recorded in each infrared imageinto a depth map 102, such as based on the density or displacement ofdots across each infrared image. The IR projector may comprise an IRlaser or diode. U.S. Pat. No. 8,374,397, which is incorporated byreference in its entirety, is one example of this IR depth technology.Therefore, during operation of the computing device 100, the depthimaging system can output a sequence of depth maps 102, wherein eachdepth map 102 contains a representation of distances between the IRcamera 122 and surfaces within the infrared field of view at acorresponding time. Of course, other depth cameras besides IR basedcameras may also be used, including but not limited to other types ofstructured like cameras, stereoscopic cameras where stereo triangulationmay be used on the stereoscopic image pairs to determine distance, depthof focus cameras, and other known types of depth cameras. In somevariations, the depth imaging system 122 may include a color camerasystem 308 which may be used instead of internal color camera system ofthe computing device.

The color imaging system may include a color camera 120, such as a CCDor CMOS camera supporting red, green, and blue color channels. The colorcamera 120 may also define a color field of view that is substantiallysimilar to (i.e., substantially overlaps) the infrared field of view ofthe IR camera 122 (and therefore the projection field of view). Asdescribed below, the computing device 100 can trigger or activate thedepth imaging system 122 and the color imaging system 120 to generate adepth map 102 and to capture a color image 110, respectively, duringeach sampling period during executing of the method, such as at a rateof 30 Hz. In other examples, the sampling rate of the camera(s) may bein the range of about 0.1 Hz to about 1 kHz, or about 60 Hz to about 240Hz. The computing device 100 can thus capture one depth map 102 and onecolor image 110 (a “frame pair”) during each sampling period and processboth depth and color data for each sampling period to detect thepresence of a surgical sponge or other surgical textile 106 in the fieldof view of the computing device 100 at the corresponding time.Alternatively, the computing device 100 can sample the depth imagingsystem and process depth map data to detect surgical sponges or surgicaltextiles in the field of view 108 of the computing device 100, and thecomputer system 100 can capture a color image 110 through the colorimaging system once a value in the frame counter 114 reaches a thresholdvalue 116, as described below. In still other embodiments, the ratio ofthe depth images 102 to color images 110 may be fixed or pre-determined,and in the range of about 3:2 to about 100:1, or about 2:1 to about50:1, or about 30:1 to about 50:1.

The computing device 100 may also include a display 118 adjacent the IRand color camera 122, 120. The display 118 can define a viewing areasubstantially normal to the fields of view of the IR and color camerassuch that a user (e.g., a nurse, a technician, an anesthesiologist)holding a surgical sponge can stand in front of the IR and color cameras122, 120 while viewing content on the display 118. For example, asdescribed below, the display 118 can render any one or more of a) anindicator that the sponge was detected, b) an indicator that an image ofthe sponge was recorded, c) a value on the sponge counter; and d) aprompt to manipulate the sponge before an image is captured, etc.substantially in real-time. In one example, the computing deviceincludes: a tablet computer including a forward-facing color camera andan integrated display; and an IR projector and IR camera mounted to thetablet, facing outwardly from the tablet, and defining projection andinfrared fields of view substantially similar to the color field of viewof the color camera. However, the computing device can include any otherintegrated or connect optical, imaging, and/or processing componentsarranged in any other suitable way.

4. Exemplary User Experience

In one example, the computing device 100 is installed in an operatingroom and executes the method depicted in FIG. 1, in the form of a nativeblood loss monitoring application utilized during an operation, surgeryor procedure. In this example, the computing device 100 continuallycaptures infrared 102 and/or color images 110 of its field of view 108and discards these images if no surgical sponge 106 a is detected in theimages or frames. The computing device 100 may also renders these framesor images on the display 118 substantially in real-time. The renderedimages are typically the color images 110, but may also be the depthimage 102 or a composite image of the color and depth images. During theoperation, a user (e.g., a nurse, a technician, an anesthesiologist) mayhold a surgical sponge 106 a in front of the imaging system 104. Withthe surgical sponge 106 a now in the field of the view 108 of theimaging system 104, the imaging system 104 captures a first depth map102 and/or a first color image 110 (a “first frame pair” or “frame set”if more than two grouped images or maps) during a first sampling periodfollowing the presence of the surgical sponge 106 a in the field of view108 of the computing device 100 in S110. The computing device 100 thenimplements machine vision techniques described herein to correlate aregion of the first depth map 102 (and a corresponding region of thefirst color image 110) with a surgical sponge 106 a and indexes a framecounter 114 from “0” to “1” in S112. In response to detecting thesurgical sponge image 106 b in the first depth map 102 (or in the firstcolor image 110), the computing device 100 renders the first infraredimage 102 (or the first color image 110) on the display 118 with acolored (e.g., green, red, yellow or other distinctive color) line orshape overlay 400 of a first width along the perimeter of the detectedsurgical sponge and/or a colored overlay area of a first opacity overthe detected area of the surgical sponge.

In the succeeding sampling period, the imaging system 104 captures asecond depth map 102 and/or a second color image 110 (a “second framepair” or “second frame set”), and the computing device 100 againimplements machine vision techniques to correlate a region of the seconddepth map 102 (and a corresponding region of the first color image 110)with the surgical sponge 106 a and indexes the frame counter 114 from“1” to “2.” In response to detecting the surgical sponge image 106 b inthe second frame pair, the computing device 100 renders the secondinfrared image 102 on the display with a broader colored line or shapeoverlay of a second width or line length 402—greater or different thanthe first width or line length—along the perimeter of the detectedsurgical sponge 106 b and/or a colored overlay area of a secondopacity—greater or different than the first opacity—over the detectedarea of the surgical sponge 106 b.

The computing device 100 can repeat this process to capture frame pairsduring subsequent sampling periods, to detect surgical sponges 106 b inthe frame pairs, to index the frame counter 114 accordingly, and torefresh the display 118 with a current depth map 102 (or color image110) with overlay perimeter and/or overlay area of line width 400, 402and opacity, respectively, representative of the frame counter value. Todynamically demonstrate the process of confirming the presence of thesurgical textile 106 b in the images 102, 110, increasing greater widthsof overlays or other changing indicia may be provided. For example, thecolor of the overlay may also change from red to yellow to green. Oncethe value on the frame counter 114 reaches a threshold value, (e.g.,“7”), the computing device captures a color image through the colorcamera, renders a visual indicator that the color image was captured onthe display, and resets the frame counter to “0” without additionalmanual input. For example, for the imaging system operating at 30 Hz andfor a preset threshold value of “7” set for the frame counter, thecomputing device can perform the forgoing methods and techniques todetect, confirm, and capture an image of a surgical sponge in less than0.3 second from entry of the surgical sponge into the field of view ofthe computing device. In other examples, the threshold value may be setin the range of about 5 to 100, or about 5 to 50, or about 4 to about30, or about 20 to about 40. The computing device may also be furtherconfigured to perform the analysis for the removal of the surgicaltextile 106 a from the field of view 108 as described in S500 and FIG.5.

The computing device 100 may be configured to perform the methods andtechniques described in U.S. patent application Ser. No. 13/544,664 totransform color values of pixels in the image into an estimation ofblood component quantity in the imaged surgical sponge in Block S140. Inresponse to confirmation of the surgical sponge 106 b in the field ofview 108 of the computing device 100 and capture of the color image 110of the surgical sponge 106 a, the computing device 100 may also index asponge or surgical textile counter 112 in Block S150 in order tomaintain a total count of surgical sponges passing the computing device100 during the operation or procedure.

5. Classifier

Block S110 of the method recites, at a first time point, capturing afirst image 102 of a field of view 108. Generally, during each samplingperiod, the computing device 100 functions to capture an infrared image102 and/or a color image 110 through the imaging system 104 in S110. Asdescribed above, the computing device 100 may also transforms theinfrared image 102 into, or to extract therefrom, a depth map of itsfield of the view. The computing device 100 can repeat this process overtime during its operation, such as at a sampling rate (or “frame rate”)of 30 Hz, or other sampling rate as described herein. However, thecomputing device can capture depth and color data of its field of viewat any other sampling rate in any other way and through any othersuitable type of sensor in Block S110.

After acquiring the image(s) 102 and/or 110, in S111 the computingdevice 100 analyzes the image(s) 102 and/or 110 to determine thepresence of one or more image characteristics therein, or to otherwiseclassify the image(s) 102 and/or 110 captured in the current samplingperiod as either containing a sponge or surgical textile 106 b, or notcontaining a sponge or surgical textile 106 b. Based upon thisdetermination, the computing device 100 may then index the frame counterin S112, or clear the frame counter in S130, respectively. Inparticular, the computing device 100 can apply one or more classifiersto a depth map 102 and/or a color image 110 captured during a samplingperiod to determine if a surgical sponge or textile 106 a is present oris not present in the field of view 108 of the computing device 100during the sampling period and to manipulate the frame counter 114accordingly, as shown in FIGS. 1 and 2.

In one exemplary method S200, the computing device 100 captures an IRand/or color image 102, 110 as in S110 of FIG. 1, and then optionallytransforms image 102 and/or 110 into a depth map in S210. In someexamples, transformation may not be needed, as the IR “image” that isoutput from the IR imaging system 122 is a depth map, or the depth mapmay be extracted from the alpha channel (or other channel) of theinfrared image, without any transformation or calculation needed. InS220, the computing device 100 applies a perimeter classifier to thedepth map captured during a sampling period to correlate an area in thedepth map with a possible surgical sponge. In one example, to compensatefor a surgical sponge that may not be held in a position substantiallynormal to the infrared camera, the computing device can scan the depthmap—along both an X-axis and a Y-axis of the depth amp—to identifychanges in depth along the Z-axis in the depth map exceeding a thresholdof 10% or more, 20% or more, 30% or more, or 40% or more, across a lineof 10 contiguous pixels. In this example, the computing device 100 cancorrelate each short, contiguous line of pixels across which a depthvalue exceeds 10% with an edge condition and then assemble adjacent andsimilar edge conditions within the depth map into perimeters of discretesurfaces within the field of view of the computing device. Once thesediscrete surfaces are thus detected, the computing device can implementtemplate matching, surface mesh, or other machine vision techniques toidentify a discrete, approximately rectilinear surface within the depthmap with a possible surgical sponge. The computing device may thus scanthe depth map for an area bounded by an approximately rectilinearperimeter characterized by a sharp increase in depth (from the imagingsystem) from the interior of the area to the exterior the area. In thisimplementation, the computing device may implement a geometry classifierthat compensates for compliance (e.g., non-rigidity) of surgicalsponges, including curvature of one or more sides of a rectilinearsponge when held vertically in front of the imaging system, which mayvary with volume of fluid in the surgical sponge, tension applied to thesurgical sponge by the user, etc.

In the foregoing implementation, the computing device may also rejectall detected surfaces not coincident a predefined point or region in thedepth map, such as all surfaces not containing the single pixel or smallpixel cluster at the lateral and longitudinal center of the depth image.The computing device may thus apply a 2D position classifier to thedepth map to reject surfaces not substantially centered in the field ofview of the imaging system. However, the computing device may implementany other geometry classifier in any other way to detect anapproximately rectilinear perimeter of a contiguous surface in the depthmap and to correlate this surface with a possible surgical sponge.

In other examples, the perimeter detection may be set to identify moreabrupt changes or decreases in the depth, e.g. more than 15%, 20%, 30%,40%, 50%, 60% or 70%, for example. Although the perimeter detection maybe performed for all four edges of a square or rectangular surgicaltextile, in other examples, the computing device 100 may only performedge scanning to the X-axis or Y-axis for depth changes, but not theother axis, and then extrapolate the edges along the other axis byconnecting the end points of the edges with an extrapolated edge. Thus,in some variations, only the top and bottom edges may be detected andthe lateral edges may be extrapolated from the ends of the top andbottom edges. Alternatively, the lateral edges may be detected and thetop and bottom edges are extrapolated.

In another implementation, the computing device 100 applies in S230 anoptional planarity classifier to a selected surface in the depthmap—correlated with a possible surgical sponge or textile, as describedabove—to determine or confirm that the selected surface is sufficientlyplanar to indicate a surgical sponge or textile 106 a. In thisimplementation, the computing device 100 can select a set of pixels(e.g., three, four, five, six, or ten) in the depth map, map a virtualplane to the set of pixels, and then calculate a histogram of normaldistances from the virtual plane to other pixels within the depth mapcorresponding to the selected surface. Thus, if the histogram indicatesthat the selected surface remains within a threshold distance of thevirtual plane across its height and width (with optional removal ofoutliers to reduce skewing), the computing device 100 can determine orassess whether the selected surface is of sufficient planarity toindicate a surgical sponge held from its upper corners. However, if thehistogram indicates that regions of the selected surface breach athreshold distance from the virtual plane, the computing device 100 candiscard the selected surface as not corresponding to a surgical spongeheld from its upper corners. In this implementation, the computingdevice can implement a threshold distance that compensates for folds,creases, and/or ripples in a surgical sponge, such as a thresholddistance of ±0.1″, ±0.25″, ±0.5″, ±0.75″, or ±1″. In thisimplementation, if the selected surface is rejected under the planarityclassifier, the computing device can generate a textual and/or graphicalprompt to stretch the surgical sponge in order to pass the planarityclassifier, and the computing device can render this prompt on thedisplay substantially in real-time.

In yet another implementation, the computing device applies a normalityclassifier in S240 to the depth map to confirm that the selected surfaceis sufficiently normal to the field of view of the imaging system toqualify for imaging and processing in Block S140 of FIG. 1. For example,the computing device 100 can calculate a virtual ray normal to thevirtual plane described above, reject the selected surface if thevirtual ray forms a maximum angle to a center of the field of view ofthe imaging system that exceeds a threshold angle, and pass the selectedsurface if the maximum angle formed between the virtual ray and thefield of view of the imaging system remains within the threshold angle.In alternate method S600, depicted in FIG. 6, after applying thenormality classifier S240, instead of the rejecting images that are notsufficiently normal to the computing device 100 or optical system 104,the computing device 100 may computationally deskew or dewarp the depthmap in S602. To dewarp the depth map, the computing device 100 maydetect the four corners and/or four edges of the surgical textile 106 bin the image 102, and apply a 3D rotational or translational matrix tonormalize the corners or edges to the same plane in the Z-axis.

After dewarping, the computing device 100 may reapply a planarityclassifier to the dewarped surgical textile 106 b, and then eitherreject the selected surface if the maximum variation in distance valuesfor pixels across the selected surface in the dewarped depth imageexceeds a threshold distance, accounting for folds, creases, and/orripples in a surgical sponge, or pass the selected surface if themaximum variation in distance values for pixels across the selectedsurface in the dewarped depth image remains within the thresholddistance, to continue further classification and/or processing using thedewarped depth image. The threshold distance may be in the range ofabout −1 cm to about +1 cm, about −2 cm to about +2 cm, or about −3 cmto about +3 cm, or about −4 cm to about +4 cm. If the dewarped imagefails the planarity classifier S604 after dewarping in S602, thecomputing system 100 may then reset the frame counter in S130 with orwithout providing an indicia or message on the display 118 of thecomputing device 100 to attempt to reposition the surgical textile 106 ain the field of view 108 in a relatively more normal orientation.Alternatively, if the selected surface is rejected under the normalityclassifier, the computing device may generate a textual and/or graphicalprompt in order to adjust the surgical sponge to pass the normalityclassifier for an additional specified number of frames, and thecomputing device can render this prompt on the display substantially inreal-time. The number of frames may be in the range of about 15 framesto 120 frames, or about 30 frames to about 60 frames, for example.

Referring back to method S200 in FIG. 2, the computing device mayoptionally apply a distance classifier S250 to the depth map to confirmthat the selected surface is within a proper depth of the imaging system104. For example, once the computing device 100 determines that theselected surface is sufficiently planar and sufficiently normal to thefield of view of the imaging system in S230 and S240, respectively, thecomputing device 100 may reject the selected surface if more than aminimum number (e.g., 1%) of pixels in the depth image 102 representingthe selected surface of the surgical textile 106 b fall outside of apreset depth range (e.g., 0.5 meter to 1.25 meters, or 30 cm to about100 cm, or about 40 cm to about 75 cm) from the imaging system 104. Inthis implementation, if the selected surface is rejected under thedistance classifier at S250, the computing device 100 may optionallygenerate a textual and/or graphical prompt on the display 118 to movethe surgical sponge 106 a closer or farther from the optical system 104of the computing device 100, in a further attempt to pass the distanceclassifier S250. The computing device 100 can render this prompt on thedisplay 118 substantially in real-time.

In the foregoing implementation, the computing device 100 may alsotransform a pixel length and a pixel width of the selected surface inthe depth image into a real length and a real distance based on distancevalues of pixels in the depth image. The computing device may thenreject the selected surface if either the real length or the real widthof the selected surface falls outside of a preset length range or apreset width range, respectively, or to confirm that such surgicaltextiles are being used. The preset dimensions for the surgical textilesmay include 2″×2″, 3″×3″, 4″×4″, 4″×8″, 4″×12″, 4″×16″, 4″×18″, 12″×12″,16″×16″, 16″×24″, 18″×30″, 15″×24″, 16″×23″, 12″×13″, 13″×18″, 24″×24″,36″×8″, 36″×36″ and the like. For each sponge type, a user may enter thesponge type and/or size at the start of the surgery or procedure, andcomputing device 100 may be configured to detect the dimensions of thosesurgical textiles within 0.5″ or 0.75″ along a width or length fordimensions less than 5″, 8″ or 10″, and 0.5″, 1″, 1.5″ or 2″ fordimensions in greater than 8″, 10″, 12″ or 15″, for example.

In another implementation, the computing device applies a textureclassifier at S260 to the depth map in order to determine if the realtexture of the selected surface represented in the depth map correspondssufficiently to a surgical textile. In one example, the computing device100 may be configured to project or define pixel clusters (e.g.,25-pixel by 25-pixel clusters) in the depth map—corresponding to theselected surface—onto a virtual plane and then apply machine visiontexture analysis methods and techniques to quantify the texture of thenormalized region of the depth map corresponding to the selectedsurface. Thus, if the quantitative value of the texture of the selectedsurface falls within a single value range or multiple distance valueranges representative of dry surgical sponges, damp surgical sponges,and saturated surgical sponges, the computing device can accept theselected surface. Otherwise, the computing device can reject theselected surface. In other examples, a Fast Fourier Transformation orwavelet transformation may be applied to the textile 106 b in theimage(s) 102, 110, to evaluate the frequency domain of the textile inone or more image channels, e.g. a RGB or depth channel. In somevariations, if the detected texture characteristic matches a surgicaltextile in the library of the computing device 100 but does not matchthe surgical textile(s) selected by the user at the start of the surgeryor procedure, the computing device 100 may prompt the user to confirmwhether a new or different surgical textile should be indicated as beingused, and may prompt the initialization or activation of a differentsurgical textile counter for that surgical textile.

In another implementation, the computing device 100 applies a colorclassifier S270 to the color image 110 in order to confirm that theselected surface contains one or more colors representative of a dry orbloodied surgical sponge. In one example, the computing device 100accepts the selected surface if at least a threshold proportion (e.g.,70%) of pixels within a region of the color image corresponding to theselected surface contain a color within either a range of red values(e.g., [ff 00 00] to [ff 40 00]) or a range of near-white values (e.g.,around [ff ff ff]), as shown in FIG. 1. Otherwise, the computing devicecan reject the selected surface.

However, the computing device 100 may also apply any other classifierparameter to the frame pair and/or to one or more selected surfaceswithin the depth map or color image in each frame pair. Duringoperation, the computing device 100 may thus apply one or moreclassifier parameters to a current frame pair and can confirm a selectedsurface within the frame pair as representative of a surgical sponge ifall applied classifier parameters pass the selected surface or pass theselected surface with sufficient confidence. Alternatively, thecomputing device 100 can confirm a selected surface within the framepair as representative of a surgical sponge if at least a thresholdnumber of applied classifier parameters pass the selected surface or atleast a threshold confidence is reached by summing the results of allapplied classifier parameters. The computing device can thus index theframe counter in Block S112, such as from “0” to “1” or from “4” to “5”.In some further variations, the user may adjust the sensitivity and/orspecificity of the computing device 100 via the user interface byadjusting the number or weight of classifiers that are applied or whichare required to pass an image pair or image set.

Otherwise, if the foregoing conditions are not met, the computing device100 may discard the frame pair as not containing an area representativeof a surgical sponge 106 b and reset the frame counter 114 to “0” inBlock S130. The computing device 100 may also discard the frame pair andreset the frame counter to “0” if the surface selected in the currentframe pair differs significantly in position, size, texture, depth, etc.from the surface selected in the preceding frame pair. For example, evenif a surface possibly indicative of a surgical sponge is detected in acurrent frame pair, the computing device can reject the current framepair and reset the frame counter if the center of the selected surfacein the current frame pair is offset from the center of a selectedsurface in the preceding frame pair by more than 0.5″ in any dimension.The computing device can thus reject surgical sponges and other surfacesmoving through the field of view of the imaging system and only confirmany image sponge samples that are held substantially static within thefield of view of the imaging system.

Although the classifiers S230, S240, S250, S260, S270 are depicted inS200 performed in a particular order, one of skill in the art willunderstand that a different order of these and other classifiers may beused, or that one more classifiers may be performed in parallel, such asin a multi-core and/or multi-threaded processor of the computing device100.

6. Sponge Confirmation

Subsequently, in response to the frame counter 114 containing a valueequivalent to a threshold value 116, the computing device records acolor image 110 of the field of view 108 and clears the frame counter114 in Block S130, either before or after further processing of theimage 110 to estimate the blood content. Generally, for each frame pairin a sequence of frame pairs, the computing device 100 analyzes a framepair independently of the preceding frame pairs to identify a surgicalsponge or textile 106 b in a frame pair or to confirm that a surgicalsponge or textile 106 b is not present in the frame pair and indexes orclears the frame counter accordingly, as shown in FIGS. 1 and 2. Whenthe frame counter 114 contains a value equivalent to the threshold value116, a total number of contiguous frame pairs equivalent to thethreshold value have been determined to include a surgical sponge, ortextile 106 b and the computing device 100 may then confirm that asurgical sponge or textile 106 a exists in the field of view 108 of theimaging system 104 and that its area in the field of view is known to asuitable degree of confidence once the frame counter 114 contains avalue equivalent to the threshold value 116.

The computing device can implement a static, preset threshold value,such as one of “7,” “10,” or “15” or otherwise be in the range of about5 to 100, or about 10 to 70, or about 30 to 50. Alternatively, thecomputer system can implement a custom threshold value set by the user.For example, the user can decrease the threshold value in order toreduce a time confirm and process an image of a surgical sponge, theuser can increase the threshold value in order to reduce false positivedetections of surgical sponges in the field of view of the imagingsystem. In still other variations, the computing device may comprise adiscontinuity counter that during a surgery or procedure, for eachinstance where a certain minimum number of continuous frames is met, butwhere threshold number of frames is not met. Depending on the value ofthe discontinuity counter over time, the computing device may adjust thethreshold value up or down, to alter the sensitivity of the detectionmethod, which may accommodate location lighting or other environmentalconditions that may affect the accuracy of the method S100.

Once the computing device thus confirms the presence of a surgicalsponge 106 a in its field of view 108, the computing device 100 mayrecord a last depth map 102 and/or color image 110 captured by theimaging system, or may trigger the imaging system to capture a new depthmap 102 and/or color image 110. The computing device 100 may thenprocess this image pair, as described below.

In some variations, to reduce the risk of inadvertently recounting orre-analyze the surgical textile 106 a that was just presented to theoptical system 104, before resetting the frame counter 114 in S130 orbefore reinitiating scanning for a new surgical textile 106 a in S110,the computing device may be further configured to detect that thesurgical textile 106 a has been removed from the field of view 108,before acquiring images to identify the next surgical textile 106 a, asshown in S500 of FIG. 5. After determining the estimated blood contentS140 and/or incrementing the textile counter 112 in S150, in S510 thecomputing device 100 may acquire a new depth map 102 and/or color image110 and determine in S520 whether the surgical sponge 106 a has beenremoved from the field of view 108, or has otherwise not been detectedin the image 102 or 110. If a surgical textile 106 b is still present inthe image 102 or 110, the user has not yet removed the prior surgicaltextile, or has not yet removed the surgical textile for a sufficientnumber of images or frames, and the computing device resets the “notextile” counter to zero.

If no surgical textile 106 b is identified in the frame or image, inS540 the “no textile” counter is incremented and then the counter ischecked against a “no textile” threshold value to determine whether asufficient number of consecutive “no textile” frames or images have beenidentified. If the threshold value has been met, the “no textile”counter may be reset and the computing device may then reset the framecounter S130. In some examples, the “no textile” threshold value may bein the range of about 5 to 100, or about 5 to 50, or about 4 to about30, or about 20 to about 40. The “no textile” threshold value in S500may be the same or may be different from the threshold value 116 in S100of FIG. 1.

7. Dynamic Classifier

In one implementation, the computer system applies the same ordered setof classifier parameters to each frame pair captured throughout itsoperation. Alternatively, the computer system can apply a set ofclassifier parameters to a frame pair based on a current value in theframe counter. For example, the computing device 100 may apply aperimeter classifier and a lateral/longitudinal position classifier to aframe pair when the frame counter contains a value of “0”, and thenapply a perimeter classifier and a normality classifier to a frame pairwhen the frame counter contains a value of “1”. The perimeter classifierand the distance classifier may be applied to a frame pair when theframe counter contains a value of “2” or more, the perimeter classifierand a texture classifier may be applied to a frame pair when the framecounter contains a value of “6”, the perimeter classifier and a colorclassifier may be applied to a frame pair when the frame countercontains a value of “7”. However, the computing device can apply anyother single or combination of classifier parameters to a frame pair toidentify a surgical sponge in the frame pair or to discard the framepair. In some other variations, the perimeter and/or position classifiermay be applied to every frame, while the remaining classifiers areapplied at different frames. In some variations, the different framesfor the remaining classifiers are pre-determined, while in othervariations, the different frames may depend on the processing time orcompletion of previous classifiers.

8. User Interface

Block S120 of the method recites rendering a form of the first image ona display, and Block S122 of the method recites, on the display,highlighting a region of the first image corresponding to the firstsurface. Generally, the computing device renders a form of the depth map(or the color image) from a current frame pair (i.e., a frame pairmost-recently captured by the imaging system) on the display in BlockS120 and renders a virtual overlay over the depth map in Block S122 tovisually indicate that a surface possibly corresponding to a surgicalsponge was detected in the frame pair as shown in FIG. 1.

In one implementation, the computing device dewarps depth maps andrenders these dewarped depth maps on the display substantially inreal-time. As each depth map is processed, as described above, thecomputing device can identify a region (e.g., a bounded area) with adepth map that may correspond to a surgical sponge and then render avisual indicator of this possible surgical sponge over the correspondingdepth map on the display substantially in real-time. For example, thecomputing device can overlay a colored outline over the perimeter of thepossible surgical sponge in the depth map rendered on the display. Inthis example, the computing device can set a line width of the outlineproportional to the current value on the frame counter. Similarly, thecomputing device can set a color of the outline based on the currentvalue on the frame counter, such as red when the current value on theframe counter is “0,” orange when the current value on the frame counteris “2,” yellow when the current value on the frame counter is “4,” andgreen when the current value on the frame counter is “6.” In anotherexample, the computing device can overlay a translucent colored areaoverlay across a region of the depth map—rendered on thedisplay—corresponding to the possible surgical sponge. In this example,the computing device can set an opacity of the area overlay proportionalto the current value on the frame counter, such as 12% opacity when thecurrent value on the frame counter is “0,” 24% opacity when the currentvalue on the frame counter is “1,” 36% opacity when the current value onthe frame counter is “3,” . . . and 84% opacity when the current valueon the frame counter is “7.” Similarly, the computing device can set acolor of the area overlay based on the current value on the framecounter, such as described above.

Therefore, in Blocks S120 and S122, the computing device can providereal-time visual feedback regarding detecting of a surgical sponge inthe field of view of the imaging system. The computing device canadditionally or alternatively implement any of the foregoing methods andtechniques to render color images and/or overlays on the displaysubstantially in real-time to provide such feedback to a user.

9. Mask

Once the presence of a surgical sponge or textile 106 b is thusconfirmed in the image 102 and/or 110, the computing device 100 mayapply an image mask or impose a perimeter of a selected and confirmedarea in the depth map onto the corresponding color image in the sameframe pair to select a region of the color image to process in BlockS140 and/or Block S150.

In some variations, to facilitate computational speed, efficiency and/oraccuracy, a method S700 to create and apply a mask to the color imagemay be optionally used. For example, in FIG. 7, the depth imaging system122 may be used to obtain a depth image S710 along with an associatedimage from the color imaging system 120. The depth channel informationis then extracted or obtained at S720, derived or calculated from theinfrared image if needed. At S730, the perimeter or edge classifier,which may be similar or the same as the perimeter or edge classifier atS220, may be used to identify the perimeter of the surgical textile. Theimage may then be deskewed or transformed at S740, if needed, to theperspective of coordinate system of the color image as describedelsewhere herein. The color image may also be processed for color and/orcontrast normalization at S750, e.g. generating a histogram distributionor color curve of the RGB channel and normalizing the color image to adifferent histogram or curve. The corresponding to the surgical textileimage is then applied as mask to the color image at S760, to exclude anybackground color pixels from unnecessary analysis.

In another example of a mask method S800, depicted in FIG. 8, a depthimage and color image are obtained from the infrared system and colorsystem at S810. At S810, a first mask is generated from the depthchannel of the infrared image by treating maximum foreground pixelvalues as positive and all other pixels as negative, which may be theresult of the surgical textile being presented to the IR camera at orbelow the IR camera's minimum depth range. At S830 and S840, the firstmask undergoes erosion and dilation, which are threshold-basedmorphological image processing operations that may be used to reducenoise and false negative pixels. For example, to perform the erosion,each pixel in the mask is replaced with the minimum value of thesurrounding pixels, which may be configured or defined as a 3×3 or 5×5,7×7, 3×5, or 5×3 pixel zone or window, for example. This erosion processmay be applied to the first mask to generate a second mask, either as asingle pass or via multiple passes, and different pixel windows may beused on different passes. This erosion process may be used reduce thebackground noise or other false positive pixels in the first mask. Next,a dilation process may be applied to the first mask to generate a thirdmask, wherein each pixel in the first mask is replaced with the maximumvalue in a group of surrounding pixels, e.g. 3×3 or 5×5, 7×7, 3×5, or5×3 pixel zone or window. The grouping may be the same or may bedifferent than the grouping used for the erosion process, and may alsobe performed in a single pass or multiple passes, with the same ordifferent grouping for each pass. This dilation process may be used topotentially turn back on certain false negative pixels. Using thesethree masks, at S850 fourth mask with 2-bit per mask pixel may beoptionally be generated wherein all pixels from the second mask areflagged as “11” or otherwise as definite foreground pixels. Any pixelsnot in the third mask are flagged as “00” or otherwise definitebackground pixels. Any pixels in the first mask but not in the secondmask are labeled “10” as probable foreground pixels, and any pixels inthe third mask but not in the first mask is labeled “01” or probablebackground pixels.

Depending upon the desired sensitivity and/or specificity needed, thefirst, second or fourth mask may be used to identify the correspondingpixels in the color image for further processing. In masks such as thefirst or fourth mask, additional processing, such as perimeter or edgedetection may be applied to further refine the mask before applicationto the color image.

10. Hand Removal

The computing device may also identify regions of the color imagecorresponding to a user's hands—holding the surgical sponge—and discardthese regions from processing in Blocks S140 and S150. For example, thecomputing device may: scan a selected region of the depth map in a framepair confirmed as representative of a surgical sponge; correlate an areawithin the depth image proximal a corner of this selected region andexhibiting reduced distance from the imaging system with a hand; andthen designate the corresponding area in the color image for removalfrom processing in Block S140. The computing device may also remove thisarea from an outline of a surgical sponge shown on the display. Thecomputing device may apply the foregoing methods and techniques to aframe pair designated for processing only after a surgical sponge hasbeen confirmed in the field of view of the imaging system.Alternatively, the computing device may apply the foregoing methods andtechniques to each frame pair and to each depth image or color imagerendered on the display.

11. Blood Component Quantity and Sponge Counter

In Block S140, once a color image confirmed as containing a regionrepresentative of a sufficiently planar surgical sponge within asuitable distance of and suitably normal to the field of view of imagingsystem is captured and recorded, the computing device can implementmethods and techniques as described in U.S. patent application Ser. No.13/544,664, which is hereby incorporated by reference in its entirety,to transform color values contained in pixels in the color image into anestimation of the mass, volume, or other quantitative measurement of theamount of whole blood, red blood cells, hemoglobin, and/or other bloodcomponent in the real surgical sponge represented in the color image.

In some variations, prior to transforming pixel color values to anestimation of a blood component value, the image (with or without anymasking described herein), may also undergo ambient light correction asdescribed in U.S. patent application Ser. No. 15/154,917, which ishereby incorporated by reference in its entirety.

In Block S150, the computing device may also implement methods andtechniques as described in U.S. patent application Ser. No. 13/544,664to index a counter representative of the total number of surgicalsponges identified and counted during an operation in which thecomputing device is in operation. In this variation, the computingdevice may render a value contained in the sponge counter on the displayand update this rendered value substantially in real-time once asurgical sponge is confirmed in the field of view of the imaging system.For example, the computing device can flash an updated sponge countervalue on the display when a surgical sponge is confirmed and counted.Similarly, when a possible surgical sponge is detected in a frame pair,the computing device can overlay a next sponge counter value (i.e., acurrent sponge count+1) over a depth (or color) image rendered on thedisplay, and the computing device can increase the opacity of theoverlaid sponge counter value as the value in the frame counterincreases for subsequent frame pairs.

In another embodiment, a color image, after segmentation of the surgicaltextile, is further segmented or masked based upon the regions of imagecomprising blood, to exclude non-blood regions of the surgical sponge.This may be performed by using a rule-based algorithm below,s=r_(i,j)+g_(i,j)+b_(i,j) where r, g and b correspond to the red, greenand blue channels of the image of the pixel at i,j location in theimage:

If

$\left( {\frac{r_{i,j}}{s} < {X\bigcap\left( {\frac{g_{i,j}}{s} > {Y\bigcup\frac{b_{i,j}}{s}} > Z} \right)}} \right)\mspace{14mu}$then remove or mask p_(i,j), else include,Where X is in the range of about 105 to about 150, Y is in the range ofabout 60 to about 70, and Z is in the range of about 60 to about 70.12. Vocal Sponge Count

In one variation, the computing device may capture and store audio datawith images and blood component quantity data for surgical spongesdetected and imaged during operation.

In particular, the computing device can record users (e.g., two users,such as nurses, anesthesiologists, technicians, etc.) sequentiallyreciting a vocalized sponge count.

In one implementation, when a possible sponge is detected in a framepair and the frame counter indexed to 1, the computing device mayinitiate an audio recording by sampling a microphone connected to orintegrated into the computing device. Subsequently, if the value of theframe counter reaches the threshold value and a surgical sponge thusconfirmed, the computing device can continue the audio recording untilthe earlier of five seconds after: the sponge is confirmed; and a newsponge is detected in the field of view of the imaging system. Thecomputing device can then store and link this audio recording with thecorresponding color image of the surgical sponge. For example, thecomputing device can record a color image of a surgical sponge,transform the color image into an estimation of a blood componentquantity (e.g., a volume of hemoglobin) in the surgical sponge, andstore this color image and the blood component quantity estimation witha time the image was captured, a sponge counter value for the surgicalsponge, and an audio recording of two users reading and confirming thecount value of the sponge.

In another implementation, the computing device may record a singleaudio track throughout an operation and then splice the audio track intomultiple discrete audio segments, match each audio segment to a recordedcolor image and a blood component quantity estimation based on a time ofthe audio segment and a time the color image was captured, and thenstore each audio segment with a tag or other pointer to itscorresponding color image or related data.

12. Duplicate Sponge Rejection—RFID

In one variation, the computing device further includes aradio-frequency identification (“RFID”) reader and RFID antenna. In thisvariation, once the computing device indexes the image counter to “1”(or to some other value less than the threshold value) to indicate apossible surgical sponge in the field of view of the imaging system, thecomputing device can broadcast an excitation signal through the RFIDantenna and then sample the RFID reader. If the sponge in the field ofthe view of the imaging system includes an RFID tag, this RFID tag canbroadcast a data packet back to the RFID reader. The computing devicecan apply receipt of this data packet from the surgical sponge toconfirm the sponge and then capture and process the color image of thesponge as soon as planarity, distance, position, and/or otherrequirements are met, as described above, and before the image counterreaches the threshold. The computing device can additionally oralternatively implement supervised machine learning techniques to trainoptical sponge detection models based on this RFID data packet receivedfrom the surgical sponge and depth maps and/or color images of thesurgical sponge. Alternatively, the computing device can broadcast anexcitation signal and read an incoming data packet from a nearby spongeonly once the frame counter reaches the threshold value and the surgicalsponge is thus confirmed optically.

In the foregoing implementation, the computing device may compare anRFID data packet received from a current surgical sponge to data packetspreviously received from other sponges during an operating period inorder to detect a duplicate scan of the same surgical sponge. Inparticular, if the RFID data packet received from the surgical sponge isidentical to an RFID data packet previously received during the sameoperating period, the computing device can reject the surgical sponge asa duplicate, discard the corresponding frame pair, and discard a bloodcomponent quantity estimation for the surgical sponge.

Furthermore, in this variation, in order to prevent detection of othernearby RFID tags, the computing device can vary the power output of theRFID antenna according to a distance between the computing device andthe sponge estimated from a current depth map. In particular, thecomputing device can translate a distance value in a region of thecurrent depth map corresponding to a possible or conformed surgicalsponge into a power level of an excitation signal to be subsequentlybroadcast by the RFID antenna. However, in this variation, if no datapacket is received following transmission of an excitation signal, thecomputing device can proceed according to Blocks of the method describedabove in order to confirm the surgical sponge and to process a colorimage of the sponge. Furthermore, if an RFID data packet is not receivedfollowing broadcast of an excitation signal, the computing device cantag the surgical sponge (e.g., the sponge counter value of the surgicalsponge, the color image of the surgical sponge, etc.) as notRFID-enabled.

In further examples, the computing device may also identify any barcode,QR code or other visual code on the surgical textile. For example, theprocessor may scan the color image for the four corners of the QR codeor barcode, and then identify the coded region. At block S410, theprocessor then decodes the coded region to determine the code string.The code string may then be used to uniquely identify the detectedsurgical textile, to avoid double-counting if the same surgical textileis presented again to the system, and to provide a warning to the useror surgeon.

13. Duplicate Sponge Rejection—Reflective IR Coating

In another variation, the computing device implements machine visiontechniques to detect a reflective material on a surgical sponge depictedin a frame pair and identify the sponge (uniquely) based on the detectedreflective material. For example, the computing device can include asecond IR emitter configured to illuminate the field of view of the IRcamera with electromagnetic radiation both reflected by material printedonto or sewn into surgical sponges and detected by the IR camera. Duringa sampling period, the computing device can thus capture and process asecond infrared image to detect a standard or substantially uniquepattern of reflective material within a surgical sponge in the field ofview of the imaging system. The computing device may then implementmethods and techniques described above to confirm presence of a surgicalsponge in the field of view of the imaging system, to uniquely identifythe image based on the pattern of reflective material, to rejectduplicate surgical sponges, to trigger early capture and processing of acolor image of the surgical sponge, and/or to improve an opticalsurgical sponge detection model according to supervised machine learningtechniques, etc.

The systems and methods described herein can be embodied and/orimplemented at least in part as a machine configured to receive acomputer-readable medium storing computer-readable instructions. Theinstructions can be executed by computer-executable componentsintegrated with the application, applet, host, server, network, website,communication service, communication interface,hardware/firmware/software elements of a user computer or mobile device,wristband, smartphone, or any suitable combination thereof. Othersystems and methods of the embodiment can be embodied and/or implementedat least in part as a machine configured to receive a computer-readablemedium storing computer-readable instructions. The instructions can beexecuted by computer-executable components integrated bycomputer-executable components integrated with apparatuses and networksof the type described above. The computer-readable medium can be storedon any suitable computer readable media such as RAMs, ROMs, flashmemory, EEPROMs, optical devices (CD or DVD), hard drives, floppydrives, or any suitable device. The computer-executable component can bea processor but any suitable dedicated hardware device can(alternatively or additionally) execute the instructions.

In the present description, the terms component, module, device, etc.may refer to any type of logical or functional circuits, blocks and/orprocesses that may be implemented in a variety of ways. For example, thefunctions of various circuits and/or blocks can be combined with oneanother into any other number of devices. Or, the devices can compriseprogramming instructions transmitted to a general purpose computer or toprocessing/graphics hardware via a transmission carrier wave. Also, thedevices can be implemented as hardware logic circuitry implementing thefunctions encompassed by the innovations herein. Finally, the devicescan be implemented using special purpose instructions (SIMDinstructions), field programmable logic arrays or any mix thereof whichprovides the desired level performance and cost.

Aspects of the method and system described herein, such as the logic,may also be implemented as functionality programmed into any of avariety of circuitry, including programmable logic devices (“PLDs”),such as field programmable gate arrays (“FPGAs”), programmable arraylogic (“PAL”) devices, electrically programmable logic and memorydevices and standard cell-based devices, as well as application specificintegrated circuits. Some other variations for implementing aspectsinclude: memory devices, microcontrollers with memory (such as EEPROM),embedded microprocessors, firmware, software, etc. Furthermore, aspectsmay be embodied in microprocessors having software-based circuitemulation, discrete logic (sequential and combinatorial), customdevices, fuzzy (neural) logic, quantum devices, and hybrids of any ofthe above device types. The underlying device technologies may beprovided in a variety of component types, e.g., metal-oxidesemiconductor field-effect transistor (“MOSFET”) technologies likecomplementary metal-oxide semiconductor (“CMOS”), bipolar technologieslike emitter-coupled logic (“ECL”), polymer technologies (e.g.,silicon-conjugated polymer and metal-conjugated polymer-metalstructures), mixed analog and digital, and so on

As a person skilled in the art will recognize from the previous detaileddescription and from the figures and claims, modifications and changescan be made to the embodiments of the invention without departing fromthe scope of this invention as defined in the following claims.

The preceding description of embodiments of the invention is notintended to limit the invention to these embodiments but rather toenable a person skilled in the art to make and use this invention.Variations, configurations, implementations, example implementations,and examples described herein are optional and are not exclusive to thevariations, configurations, implementations, example implementations,and examples they describe. The invention described herein can includeany and all permutations of these variations, configurations,implementations, example implementations, and examples.

What is claimed is:
 1. A system for measuring blood content, the systemcomprising: a color imaging system configured to acquire one or morecolor images of a surgical textile; an infrared imaging systemconfigured to acquire one or more infrared images of the surgicaltextile; and a processor configured to: generate a depth image of depthinformation from at least one of the one or more infrared images;identify a shape of the surgical textile using the depth image; generateshape information of the identified shape of the surgical textile fromthe depth image; use the shape information to identify surgical textilepixels that correspond to the surgical textile in the one or more colorimages; and extract blood information from the surgical textile pixels.2. The system of claim 1, wherein the processor is further configured totransform the infrared images to a coordinate system corresponding tothe one or more color images.
 3. The system of claim 1, wherein theprocessor is further configured to identify a set of pixels thatrepresent a planar surface in the depth image.
 4. The system of claim 1,wherein the processor is further configured to detect a surgical textileimage perimeter in the depth image.
 5. The system of claim 4, whereindetection of the surgical textile image perimeter is performed bylooking for a sharp vertical depth drop-off in the depth image.
 6. Thesystem of claim 1, wherein the processor is further configured todownsample at least one of the depth image or at least one of the one ormore infrared images.
 7. The system of claim 6, wherein the processor isfurther configured to generate a mask image from the downsampled depthimage.
 8. The system of claim 7, wherein the processor is furtherconfigured to upsample the mask image.
 9. The system of claim 1, whereinthe processor is further configured to perform fill-in of missinginfrared pixel region in the one or more infrared images.
 10. The systemof claim 4, wherein the processor is further configured to generate amask image using the detected perimeter.
 11. The system of claim 10,wherein the processor is further configured to transform the mask imageto a coordinate system of the one or more color images.
 12. The systemof claim 10, wherein the detected perimeter is a top edge and a bottomedge of a surgical textile image.
 13. The system of claim 10, whereinthe detected perimeter comprises opposing edges of a surgical textileimage.
 14. The system of claim 10, wherein the detected perimetercomprises corners of a surgical textile image.
 15. A method of analyzingan object containing a blood component, the method comprising: for theobject containing the blood component, acquiring both a depth image anda color image both of the object containing the blood component; usingthe depth image to detect the object in a field of view; and using thecolor image to estimate a blood component characteristic of the bloodcomponent contained in the object.
 16. The method of claim 15, furthercomprising: generating an image mask using the depth image; and applyingthe image mask to the color image to eliminate background pixels. 17.The method of claim 16, further comprising: applying at least one oferosion image processing or dilation image processing to the depthimage.
 18. A method of performing fluid monitoring, comprising:capturing an infrared image of a surgical textile in a field of view;capturing a color image of the surgical textile in the field of view;generating an image mask using the infrared image of the surgicaltextile; and using the image mask with the color image to identify aregion of the color image corresponding to the surgical textile.
 19. Themethod of claim 18, further comprising transforming the infrared imageto a geometry perspective of the color image.
 20. The method of claim18, further comprising downsampling the infrared image prior togenerating the image mask.
 21. The method of claim 20, furthercomprising upsampling the image mask before using the image mask toidentify the region of the color image.